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Summary Literature (0)
MIM:255320 - CONGENITAL MYOPATHY 1B, AUTOSOMAL RECESSIVE; CMYP1B

Xenbase Genes: ryr1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009712 - congenital multicore myopathy with external ophthalmoplegia
MONDO:0018948 - multiminicore myopathy

Disease Ontology (DO):
DOID:0080991 - congenital myopathy 1B